We comment on the conjecture by Parker et al. (2016) that Antarctic toothfish recently returned to McMurdo Sound, arguing that this species never departed. Instead, as deduced from a 40-year fishing effort, toothfish water column prevalence became markedly reduced where bottom depths are <500 m, with research continuing to show their presence on the bottom or above the bottom where depths are deeper. We also counter arguments that toothfish departed, and remained absent, during and following a five-year presence of mega-icebergs residing near the opposite coast of Ross Island, the icebergs inhibiting or fomenting conditions that discouraged toothfish presence in the Sound. Available analyses reveal that toothfish movement into the Sound was probably not significantly affected, and additionally that neither changes in hydrography nor in primary productivity in the Sound would have been sufficient to impact toothfish presence through food web alteration. We hypothesize that the local effect of predation by seals and whales and the regional effect of a fishery targeting the largest toothfish (those neutrally buoyant and thus capable of occupying upper levels of the water column) has resulted in the remaining toothfish now being found predominantly closer to the bottom at greater depths.

Evolutionary disparate Antarctic notothenioids and Arctic gadids have adapted to their freezing environments through the elaboration of essentially identical antifreeze glycoproteins (AFGPs). Here we show that this convergence of molecular identity, which evolved from unrelated parent genes, extends to convergence in physiological deployment. Both fish groups synthesize AFGPs in the exocrine pancreas from where they are discharged into the gut to inhibit the growth of ingested ice. Antifreeze glycoproteins not lost with the faeces are resorbed from the gut via the rectal epithelium, transported to the blood and ultimately secreted into the bile, from where they re-enter the gastrointestinal tract. Antifreeze glycoprotein recirculation conserves energy expenditure and explains how high levels of AFGPs reach the blood in notothenioids since, unlike Arctic gadids which also synthesize AFGP in the liver, AFGP secretion in notothenioids is directed exclusively towards the gastrointestinal lumen. Since AFGPs function by inhibiting ice crystal growth, ice must be present for them to function. The two fish groups are thus faced with an identical problem of how to deal with internal ice. Here we show that both accumulate AFGPs within ellipsoidal macrophages of the spleen, presumably adsorbed to phagocytosed ice crystals which are then held until a warming event ensues.

Antarctic fishes survive freezing through the secretion of antifreeze glycoproteins (AFGPs), which bind to ice crystals to inhibit their growth. This mode of action implies that ice crystals must be present internally for AFGPs to function. The entry and internal accumulation of ice is likely to be lethal, however, so how do fishes survive in its presence? We propose a novel function for the interaction between internal ice and AFGPs, namely the promotion of ice uptake by splenic phagocytes. We show here that i) external mucus of Antarctic notothenioids contains AFGPs and thus has a potential protective role against ice entry, ii) AFGPs are distributed widely through the extracellular space ensuring that they are likely to come into immediate contact with ice that penetrates their protective barriers, and iii) using AFGP-coated nanoparticles as a proxy for AFGP adsorbed onto ice, we suggest that internal ice crystals are removed from the circulation through phagocytosis, primarily in the spleen. We argue that intracellular sequestration in the spleen minimizes the risks associated with circulating ice and enables the fish to store the ice until it can be dealt with at a later date, possibly by melting during a seasonal warming event.

Nesting sites of the naked dragonfish Gymnodraco acuticeps have been identified in 15–35 m water under fast ice adjacent to McMurdo Station, making it possible to examine embryonic development and early larval growth. Egg-laying (predominantly in October) is preceded by a distinctive whirling behavioural pattern driven by the male prodding the side of the female's abdomen. The eggs (3.42 ± 0.19 mm in diameter) are laid on rocks as a single adherent layer (c. 2500 per patch). Development is unusually protracted, the first cleavage occurring after about 24 hr at about −1.9°C. Hatching occurs about 10 months post-fertilization, beginning soon after the sun rises above the horizon. During this period one of the parents may act as a guard in an attempt to keep predators at bay. Upon hatching, the larvae (12.09 ± 0.36 mm long) swim towards the surface ice where they presumably seek refuge. Yolk absorption is complete in about 15 days. Larvae (grown in aquaria at a density of 0.7 larvae l−1) display an average daily growth rate of 0.42% over nine weeks. Hatching in aquaria can occur up to 100 days in advance of that seen in the field, suggesting that under natural conditions hatching may be delayed until an appropriate stimulus (such as the return of the sun) is received.

A mutation of a gene (discovered in Festuca pratensis Huds. and designated sid ) confers indefinite greenness on senescing leaves. Via intergeneric hybrids with Lolium multiflorum L. and Lolium perenne L., the mutant gene (sidy) has been introgressed into a range of Lolium backgrounds. Using genomic in situ hybridization we have identified segments carrying sidy in recombinant chromosomes of Lolium–Festuca introgression lines. We also used L. perenne lines segregating 1[ratio ]1 for the staygreen character to tag the gene with molecular markers. In two mapping populations a total of 84 genotypes were screened with isoenzymes, RAPD primers, RFLP probes and AFLP primer pairs. Over 180 polymorphic loci were identified, representing 10 linkage groups spanning 600 cM. Two AFLP markers are linked to sid at 4·6 and 14·9 cM, close enough to be usable for marker-assisted selection. Introgression of sidy into Lolium temulentum L. resulted in the production of near-isogenic inbreeding lines suitable for comparative studies of gene expression. Using a variation of the method of representational difference analysis a very small number of cDNAs have been identified as promising candidates for sid, or genes directly regulated by sid.